✦ LIBER ✦

16q21 is critical for 16q deletion syndrome

✍ Scribed by K. Naritomi; N. Shiroma; Y. Izumikawa; K. Sameshima; S. Ohdo; K. Hirayama

Book ID: 115089809
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 259 KB
Volume: 33
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.1988.tb03464.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Interstitial deletion of chromosome 16q:

Interstitial deletion of chromosome 16q: 16q22 is critical for 16q- syndrome

✍ Fujiwara, Masataka ;Yoshimoto, Toru ;Morita, Yasuyuki ;Kamada, Makoto 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 339 KB 👁 1 views

Partial deletion of 16q is rare; to our knowledge only 12 cases have been published

Identical twins with deletion 16q syndro

Identical twins with deletion 16q syndrome: Evidence that 16q12.2-q13 is the critical band region

✍ F. F. B. Elder; J. W. Ferguson; L. H. Lockhart 📂 Article 📅 1984 🏛 Springer 🌐 English ⚖ 894 KB

An interstitial deletion of the long arm of chromosome 16 has been identified in identical twins. These patients are strikingly similar phenotypically to previously reported cases of deletion 16q syndrome but differ chromosomally in that their deletion involves the 16q12.2-q13 rather than the 16q21.

De novo interstitial deletion q16.2q21 o

De novo interstitial deletion q16.2q21 on chromosome 6

✍ Villa, Amelia ;Urioste, Miguel ;Bofarull, Josep M. ;Martínez-Frías, María-Luisa 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 437 KB 👁 2 views

Phenotypic variability of a deletion and

Phenotypic variability of a deletion and duplication 6q16.1 → q21 due to a paternal balanced ins(7;6)(p15;q16.1q21)

✍ Ana Spreiz; Doris Müller; Sibylle Zotter; Ursula Albrecht; Matthias Baumann; Chr 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 235 KB 👁 2 views

Physical findings in 21q22 deletion sugg

Physical findings in 21q22 deletion suggest critical region for 21q— phenotype in q22

✍ Theodoropoulos, Demetrios S. ;Cowan, Janet M. ;Elias, Ellen R. ;Cole, Cynthia 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 331 KB

Bilateral frontoparietal polymicrogyria

Bilateral frontoparietal polymicrogyria (BFPP) syndrome secondary to a 16q12.1-q21 chromosome deletion involving GPR56 gene

✍ Renato Borgatti; Susan Marelli; Laura Bernardini; Antonio Novelli; Anna Cavallin 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 709 KB